Surepulse recalls VS Cap Extra Large (REF SP-163-A1) for incorrect sizing guide on newborn heart rate monitor. This may cause improper fit. No remedy provided in official notice.
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
Surepulse is recalling the VS Cap Extra Large (REF SP-163-A1) component for newborn heart rate monitors due to an incorrect sizing guide in the labeling. This could lead to improper fit if the cap is not sized correctly for the baby's head.
The cap's labeling contains an incorrect sizing guide, which could lead to improper fit if the caregiver uses the cap without following the correct size instructions. This might cause the cap to be too loose or too tight for the baby's head.
Newborn caregivers who own the Surepulse VS Newborn Heart Rate Monitor with the specific cap model (REF SP-163-A1) are affected. The risk is low as the issue is labeling-related and not a physical hazard.
Check if your Surepulse VS Newborn Heart Rate Monitor includes the VS Cap Extra Large with reference number SP-163-A1. The product was sold with specific batch numbers listed in the recall notice.
Look for the reference number SP-163-A1 on the cap to confirm it is part of the recalled batch.
The official recall notice does not provide a remedy for this issue.
Check the reference number SP-163-A1 on the cap. The product was sold with specific batch numbers listed in the recall notice.
The recall is for labeling issues, not a physical hazard. The risk is low as the issue is about sizing instructions, not a direct safety risk.
We’ve drafted a message you can send Surepulse to request your refund or repair — edit it as you like.
Subject: Recall Z-1360-2026 — Surepulse Surepulse Hello, I own a Surepulse that is covered by recall Z-1360-2026 from Surepulse. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
